H5330

GUDID 03700393300158

Single use, hook with monopolar cautery for laparoscopic surgery

PETERS SURGICAL

Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use Endoscopic electrosurgical electrode, monopolar, single-use
Primary Device ID03700393300158
NIH Device Record Keyf78d31e3-771d-4ed4-a538-0b2776e4b3c3
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberH5330
Catalog NumberH5330
Company DUNS265741780
Company NamePETERS SURGICAL
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+33470584170
Emailvectec@vectec.fr
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com
Phone+1 508-747-6033
Emaile.knupp@peters-surgical.com

Device Dimensions

Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter
Outer Diameter5 Millimeter
Length330 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS103700393300158 [Package]
Contains: 03700393300165
Package: Box [25 Units]
In Commercial Distribution
GS103700393300165 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-09-20
Device Publish Date2016-09-12

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03661522100929 - Applier, hemostatic clip2024-01-10
03661522100936 - Applier, hemostatic clip2024-01-10
03661522100912 - Applier, hemostatic clip2024-01-05
03661522000984 - Sertilac2023-06-19
03661522039540 - Applier, hemostatic clip2023-06-16

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